Synthesis of a maradolipid without using protecting groups
2013
Csuk, René | Schultheiß, Andrea | Sommerwerk, Sven | Kluge, Ralph
A convenient route has been developed to synthesize 6-O-mono- and 6,6′-di-O-acyl symmetrical and unsymmetrical (un)-symmetrically trehalose derivatives from trehalose using a combination of enzymic and nonenzymic reactions. Thus, a typical maradolipid was accessed in two-steps.
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